MX2016007801A - Pyrimidopyrimidinones useful as wee-1 kinase inhibitors. - Google Patents

Pyrimidopyrimidinones useful as wee-1 kinase inhibitors.

Info

Publication number
MX2016007801A
MX2016007801A MX2016007801A MX2016007801A MX2016007801A MX 2016007801 A MX2016007801 A MX 2016007801A MX 2016007801 A MX2016007801 A MX 2016007801A MX 2016007801 A MX2016007801 A MX 2016007801A MX 2016007801 A MX2016007801 A MX 2016007801A
Authority
MX
Mexico
Prior art keywords
wee
useful
pyrimidopyrimidinones
kinase inhibitors
compounds
Prior art date
Application number
MX2016007801A
Other languages
Spanish (es)
Other versions
MX371108B (en
Inventor
Harrison Timothy
Trevitt Graham
Roderick O´Dowd Colin
John Wilkinson Andrew
robin hewitt Peter
Burkamp Frank
d shepherd Steven
Miel Hugues
Original Assignee
Almac Discovery Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Almac Discovery Ltd filed Critical Almac Discovery Ltd
Publication of MX2016007801A publication Critical patent/MX2016007801A/en
Publication of MX371108B publication Critical patent/MX371108B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The present invention relates to compounds that are useful as inhibitors of the activity of Wee-1 kinase. The present invention also relates to pharmaceutical compositions comprising these compounds and to methods of using these compounds in the treatment of cancer and methods of treating cancer.
MX2016007801A 2013-12-19 2014-12-19 Pyrimidopyrimidinones useful as wee-1 kinase inhibitors. MX371108B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1322602.2A GB201322602D0 (en) 2013-12-19 2013-12-19 Pharmaceutical compounds
PCT/GB2014/053793 WO2015092431A1 (en) 2013-12-19 2014-12-19 Pyrimidopyrimidinones useful as wee-1 kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2016007801A true MX2016007801A (en) 2016-09-07
MX371108B MX371108B (en) 2020-01-17

Family

ID=50071157

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2016007801A MX371108B (en) 2013-12-19 2014-12-19 Pyrimidopyrimidinones useful as wee-1 kinase inhibitors.

Country Status (27)

Country Link
US (1) US9850247B2 (en)
EP (1) EP3083625B1 (en)
JP (1) JP6437559B2 (en)
KR (1) KR102405462B1 (en)
CN (1) CN105829315B (en)
AU (1) AU2014369457B2 (en)
BR (1) BR112016014151B1 (en)
CA (1) CA2933755C (en)
CY (1) CY1120035T1 (en)
DK (1) DK3083625T3 (en)
ES (1) ES2650013T3 (en)
GB (1) GB201322602D0 (en)
HR (1) HRP20180080T1 (en)
HU (1) HUE037908T2 (en)
IL (1) IL245672B (en)
LT (1) LT3083625T (en)
MX (1) MX371108B (en)
NO (1) NO3083625T3 (en)
NZ (1) NZ720178A (en)
PL (1) PL3083625T3 (en)
PT (1) PT3083625T (en)
RS (1) RS56731B1 (en)
RU (1) RU2691105C1 (en)
SG (1) SG11201603814TA (en)
SI (1) SI3083625T1 (en)
WO (1) WO2015092431A1 (en)
ZA (1) ZA201603337B (en)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10364247B2 (en) * 2015-04-21 2019-07-30 Ruijin Hospital Affiliated To Shanghai Jiao Tong University School Of Medicine Preparation and use of novel protein kinase inhibitors
CA3003737C (en) * 2015-11-01 2021-09-14 The Regents Of The University Of Colorado, A Body Corporate Wee1 kinase inhibitors and methods of making and using the same
CN109906227B (en) * 2016-11-16 2022-03-11 上海瑛派药业有限公司 8, 9-dihydroimidazo [1,2-a ] pyrimido [5,4-e ] pyrimidin-5 (6H) -ones
WO2018124001A1 (en) 2016-12-27 2018-07-05 国立研究開発法人理化学研究所 Bmp-signal-inhibiting compound
US10954253B2 (en) 2017-01-23 2021-03-23 Shijiazhuang Sagacity New Drug Development Co., Ltd. 1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one derivative as Wee1 inhibitor
GB201703881D0 (en) * 2017-03-10 2017-04-26 Almac Discovery Ltd Pharmaceutical compounds
US20200108074A1 (en) 2017-03-31 2020-04-09 Seattle Genetics, Inc. Combinations of chk1- and wee1- inhibitors
WO2019011228A1 (en) * 2017-07-10 2019-01-17 上海瑛派药业有限公司 Imidazo[1,2-b]pyrimido[4,5-d]pyridazin-5(6h)-one compound and use thereof
WO2019037678A1 (en) * 2017-08-24 2019-02-28 上海迪诺医药科技有限公司 Pyrazolo[3,4-d]pyrimidin-3-one derivative, pharmaceutical composition and use thereof
US10807994B2 (en) 2017-10-09 2020-10-20 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
US11299493B2 (en) 2017-10-09 2022-04-12 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
AU2018361010B2 (en) 2017-11-01 2023-01-12 Wuxi Biocity Biopharmaceutics Co., Ltd. Macrocyclic compound serving as Wee1 inhibitor and applications thereof
EP3758706A4 (en) * 2018-02-28 2021-11-24 The Regents Of The University Of Colorado Wee1 kinase inhibitors and methods of treating cancer using the same
KR20210066839A (en) * 2018-09-27 2021-06-07 베타 파머수티컬 컴퍼니 리미티드 FGFR4 inhibitors and uses thereof
US20210403451A1 (en) 2018-10-26 2021-12-30 Wenyuan Qian Pyrimidopyrazolone derivative as wee1 inhibitor and use thereof
KR20210141659A (en) 2019-03-22 2021-11-23 쇼우야오 홀딩스 (베이징) 코., 엘티디. WEE1 inhibitors and their preparation and use
EP3952879A4 (en) * 2019-04-09 2023-01-04 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
CN113939296A (en) 2019-04-09 2022-01-14 诺维逊生物股份有限公司 Heterocyclic compounds and their use
WO2020210383A1 (en) * 2019-04-09 2020-10-15 Nuvation Bio Inc. Heterocyclic compounds and uses thereof
FI3964510T3 (en) 2019-04-30 2024-07-24 Wuxi Biocity Biopharmaceutics Co Ltd Crystal form of wee1 inhibitor compound and use thereof
CN112142763B (en) * 2019-06-28 2024-01-26 上海医药集团股份有限公司 Pyrazolopyrimidine compound, and preparation method and application thereof
CN115698006B (en) 2020-06-17 2024-03-29 微境生物医药科技(上海)有限公司 Pyrazolo [3,4-d ] pyrimidin-3-one derivatives as Wee-1 inhibitors
WO2022072336A1 (en) * 2020-10-01 2022-04-07 University Of Washington Drug-like molecules and methods for the therapeutic targeting of microrna-21
JP2023554430A (en) * 2020-12-18 2023-12-27 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド Nitrogen-containing 2,3-dihydroquinazolinone compounds as Nav1.8 inhibitors
WO2022228511A1 (en) 2021-04-30 2022-11-03 微境生物医药科技(上海)有限公司 Fused ring compound as wee-1 inhibitor, and preparation method therefor and use thereof
CN116462687A (en) 2022-01-18 2023-07-21 江苏天士力帝益药业有限公司 WEE1 inhibitor and preparation and application thereof
CN116836184A (en) * 2022-03-25 2023-10-03 药雅科技(上海)有限公司 Preparation and application of Wee1 kinase inhibitor
WO2023217201A2 (en) * 2022-05-10 2023-11-16 杭州德睿智药科技有限公司 Novel pyrimido-heterocyclic novel compound serving as wee1 inhibitor and application thereof

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7504396B2 (en) 2003-06-24 2009-03-17 Amgen Inc. Substituted heterocyclic compounds and methods of use
CN1930163A (en) 2004-03-15 2007-03-14 霍夫曼-拉罗奇有限公司 Novel dichloro-phenyl-pyrido [2,3-d] pyrimidine derivates, their manufacture and use as pharmaceutical agents
FR2896246B1 (en) 2006-01-13 2008-08-15 Sanofi Aventis Sa PYRIDO-PYRIMIDONE DERIVATIVES, THEIR PREPARATION, THEIR THERAPEUTIC APPLICATION
AR060635A1 (en) 2006-04-27 2008-07-02 Banyu Pharma Co Ltd DERIVATIVES OF 1,2-DIHIDRO-3H-PIRAZOLO [3,4-D] PIRIMIDIN-3-ONA, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THEM AND THEIR USE IN THE TREATMENT OF CANCER
US8198281B2 (en) 2007-04-25 2012-06-12 Merck Sharp & Dohme Corp. Crystalline forms of dihydropyrazolopyrimidinone
DK2168966T3 (en) 2007-06-15 2017-01-23 Msd Kk BICYCLOANILIN DERIVATIVES
AU2008315048A1 (en) * 2007-10-23 2009-04-30 Msd K.K. Pyridone-substituted-dihydropyrazolopyrimidinone derivative
CA2745970A1 (en) * 2008-12-12 2010-06-17 Msd K.K. Dihydropyrimidopyrimidine derivative
WO2010067888A1 (en) 2008-12-12 2010-06-17 Banyu Pharmaceutical Co.,Ltd. Dihydropyrimidopyrimidine derivatives
US20130252963A1 (en) * 2010-12-06 2013-09-26 Yun Jin Pyrimidinone compounds for use in the treatment of disease or conditions mediated by lp-pla2
WO2012085167A1 (en) * 2010-12-22 2012-06-28 Merz Pharma Gmbh & Co. Kgaa Metabotropic glutamate receptor modulators
TWI532742B (en) 2011-02-28 2016-05-11 艾伯維有限公司 Tricyclic inhibitors of kinases
EP2731953A1 (en) 2011-07-15 2014-05-21 Abbvie Inc. Tricyclic inhibitors of kinases useful for the treatment of proliferative diseases
US8796289B2 (en) 2011-07-19 2014-08-05 Abbvie Inc. Pyridazino[4,5-D]pyrimidin-5(6H)-one inhibitors of kinases
EP2776434A1 (en) 2011-10-20 2014-09-17 Abbvie Inc. Pyridopyrimidinone inhibitors of kinases
WO2013126656A1 (en) 2012-02-23 2013-08-29 Abbvie Inc. Pyridopyrimidinone inhibitors of kinases
CN102816164A (en) * 2012-08-31 2012-12-12 北京理工大学 Method for synthesizing 7-amino-2, 3-dihydropyrimido (4, 5-d) pyrimidin-4(1H)-one

Also Published As

Publication number Publication date
KR102405462B1 (en) 2022-06-03
IL245672B (en) 2021-10-31
CA2933755A1 (en) 2015-06-25
KR20160098499A (en) 2016-08-18
EP3083625B1 (en) 2017-11-01
GB201322602D0 (en) 2014-02-05
DK3083625T3 (en) 2017-12-18
MX371108B (en) 2020-01-17
US9850247B2 (en) 2017-12-26
RS56731B1 (en) 2018-03-30
AU2014369457B2 (en) 2018-08-09
JP2017500335A (en) 2017-01-05
AU2014369457A1 (en) 2016-06-09
CA2933755C (en) 2023-01-31
PT3083625T (en) 2018-02-06
IL245672A0 (en) 2016-06-30
SI3083625T1 (en) 2018-03-30
SG11201603814TA (en) 2016-07-28
LT3083625T (en) 2017-12-27
HRP20180080T1 (en) 2018-03-09
CN105829315B (en) 2019-03-08
NZ720178A (en) 2022-05-27
ES2650013T3 (en) 2018-01-16
RU2691105C1 (en) 2019-06-11
JP6437559B2 (en) 2018-12-12
HUE037908T2 (en) 2018-09-28
ZA201603337B (en) 2018-07-25
EP3083625A1 (en) 2016-10-26
BR112016014151A2 (en) 2017-08-08
PL3083625T3 (en) 2018-03-30
CY1120035T1 (en) 2018-12-12
CN105829315A (en) 2016-08-03
WO2015092431A1 (en) 2015-06-25
NO3083625T3 (en) 2018-03-31
RU2016123363A (en) 2018-01-25
BR112016014151B1 (en) 2023-01-17
US20160318936A1 (en) 2016-11-03

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